检索结果 - Isaacs, Aaron

Considerations for the Assessment of Substrates, Genetics and Risk Factors in Patients with Atrial Fibrillation 由 Linz, Dominik, Verheule, Sander, Isaacs, Aaron, Schotten, Ulrich

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Non-alcoholic fatty liver disease and cardiovascular disease: assessing the evidence for causality 由 Brouwers, Martijn C. G. J., Simons, Nynke, Stehouwer, Coen D. A., Isaacs, Aaron

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Relationship Between Nonalcoholic Fatty Liver Disease Susceptibility Genes and Coronary Artery Disease 由 Brouwers, Martijn C.G.J., Simons, Nynke, Stehouwer, Coen D.A., Koek, Ger H., Schaper, Nicolaas C., Isaacs, Aaron

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Failing beta-cell adaptation in South Asian families with a high risk of type 2 diabetes 由 Jainandunsing, Sjaam, Özcan, Behiye, Rietveld, Trinet, van Miert, Joram N. I., Isaacs, Aaron J., Langendonk, Janneke G., de Rooij, Felix W. M., Sijbrands, Eric J. G.

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New-onset perioperative atrial fibrillation in cardiac surgery patients: transient trouble or persistent problem?—Authors’ reply 由 Kawczynski, Michal J, Zeemering, Stef, Gilbers, Martijn, Isaacs, Aaron, Verheule, Sander, Zink, Matthias D, Maesen, Bart, Bramer, Sander, Van Gelder, Isabelle C, Crijns, Harry J G M, Schotten, Ulrich, Bidar, Elham

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Low Density Lipoprotein Exposure of Plasmacytoid Dendritic Cells Blunts Toll-like Receptor 7/9 Signaling via NUR77 由 Christ, Anette, Goossens, Pieter G., Wijnands, Erwin, Jin, Han, Legein, Bart, Oth, Tammy, Isaacs, Aaron, Stoll, Monika, Vanderlocht, Joris, Lutgens, Esther, Daemen, Mat J. A. P., Zenke, Martin, Biessen, Erik A. L.

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Clinical and electrophysiological predictors of device-detected new-onset atrial fibrillation during 3 years after cardiac surgery 由 Bidar, Elham, Zeemering, Stef, Gilbers, Martijn, Isaacs, Aaron, Verheule, Sander, Zink, Matthias D, Maesen, Bart, Bramer, Sander, Kawczynski, Michal, Van Gelder, Isabelle C, Crijns, Harry J G M, Maessen, Jos G, Schotten, Ulrich

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A systematic SNP selection approach to identify mechanisms underlying disease aetiology: linking height to post-menopausal breast and colorectal cancer risk 由 Elands, Rachel J. J., Simons, Colinda C. J. M., Riemenschneider, Mona, Isaacs, Aaron, Schouten, Leo J., Verhage, Bas A., Van Steen, Kristel, Godschalk, Roger W. L., van den Brandt, Piet A., Stoll, Monika, Weijenberg, Matty P.

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Heritabilities, apolipoprotein E, and effects of inbreeding on plasma lipids in a genetically isolated population: The Erasmus Rucphen Family Study 由 Isaacs, Aaron, Sayed-Tabatabaei, Fakhredin A., Aulchenko, Yurii S., Zillikens, M. Carola, Sijbrands, Eric J. G., Schut, Anna F. C., Rutten, Wim P. F., Pols, Huibert A. P., Witteman, Jacqueline C. M., Oostra, Ben A., van Duijn, Cornelia M.

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A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study 由 Silva, Claudia T., Zorkoltseva, Irina V., Amin, Najaf, Demirkan, Ayşe, van Leeuwen, Elisabeth M., Kors, Jan A., van den Berg, Marten, Stricker, Bruno H., Uitterlinden, André G., Kirichenko, Anatoly V., Witteman, Jacqueline C. M., Willemsen, Rob, Oostra, Ben A., Axenovich, Tatiana I., van Duijn, Cornelia M., Isaacs, Aaron

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A genome-wide association scan of RR and QT interval duration in three European genetically isolated populations. The EUROSPAN project 由 Marroni, Fabio, Pfeufer, Arne, Aulchenko, Yurii S, Franklin, Christopher S, Isaacs, Aaron, Pichler, Irene, Wild, Sarah H, Oostra, Ben A, Wright, Alan F, Campbell, Harry, Witteman, Jacqueline C, Kääb, Stefan, Hicks, Andrew A, Gyllensten, Ulf, Rudan, Igor, Meitinger, Thomas, Pattaro, Cristian, van Duijn, Cornelia M, Wilson, James F, Pramstaller, Peter P

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Association of the IGF1 gene with fasting insulin levels 由 Willems, Sara M, Cornes, Belinda K, Brody, Jennifer A, Morrison, Alanna C, Lipovich, Leonard, Dauriz, Marco, Chen, Yuning, Liu, Ching-Ti, Rybin, Denis V, Gibbs, Richard A, Muzny, Donna, Pankow, James S, Psaty, Bruce M, Boerwinkle, Eric, Rotter, Jerome I, Siscovick, David S, Vasan, Ramachandran S, Kaplan, Robert C, Isaacs, Aaron, Dupuis, Josée, van Duijn, Cornelia M, Meigs, James B

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Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs 由 Ricaño-Ponce, Isis, Zhernakova, Daria V., Deelen, Patrick, Luo, Oscar, Li, Xingwang, Isaacs, Aaron, Karjalainen, Juha, Di Tommaso, Jennifer, Borek, Zuzanna Agnieszka, Zorro, Maria M., Gutierrez-Achury, Javier, Uitterlinden, Andre G., Hofman, Albert, van Meurs, Joyce, Netea, Mihai G., Jonkers, Iris H., Withoff, Sebo, van Duijn, Cornelia M., Li, Yang, Ruan, Yijun, Franke, Lude, Wijmenga, Cisca, Kumar, Vinod

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A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy 由 Silva, Claudia Tamar, Zorkoltseva, Irina V., Niemeijer, Maartje N., van den Berg, Marten E., Amin, Najaf, Demirkan, Ayşe, van Leeuwen, Elisa, Iglesias, Adriana I., Piñeros-Hernández, Laura B., Restrepo, Carlos M., Kors, Jan A., Kirichenko, Anatoly V., Willemsen, Rob, Oostra, Ben A., Stricker, Bruno H., Uitterlinden, André G., Axenovich, Tatiana I., van Duijn, Cornelia M., Isaacs, Aaron

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A Genome-Wide Association Study of Optic Disc Parameters 由 Ramdas, Wishal D., van Koolwijk, Leonieke M. E., Ikram, M. Kamran, Jansonius, Nomdo M., de Jong, Paulus T. V. M., Bergen, Arthur A. B., Isaacs, Aaron, Amin, Najaf, Aulchenko, Yurii S., Wolfs, Roger C. W., Hofman, Albert, Rivadeneira, Fernando, Oostra, Ben A., Uitterlinden, Andre G., Hysi, Pirro, Hammond, Christopher J., Lemij, Hans G., Vingerling, Johannes R., Klaver, Caroline C. W., van Duijn, Cornelia M.

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A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level 由 Pattaro, Cristian, De Grandi, Alessandro, Vitart, Veronique, Hayward, Caroline, Franke, Andre, Aulchenko, Yurii S, Johansson, Asa, Wild, Sarah H, Melville, Scott A, Isaacs, Aaron, Polasek, Ozren, Ellinghaus, David, Kolcic, Ivana, Nöthlings, Ute, Zgaga, Lina, Zemunik, Tatijana, Gnewuch, Carsten, Schreiber, Stefan, Campbell, Susan, Hastie, Nick, Boban, Mladen, Meitinger, Thomas, Oostra, Ben A, Riegler, Peter, Minelli, Cosetta, Wright, Alan F, Campbell, Harry, van Duijn, Cornelia M, Gyllensten, Ulf, Wilson, James F, Krawczak, Michael, Rudan, Igor, Pramstaller, Peter P

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Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect 由 Broer, Linda, Codd, Veryan, Nyholt, Dale R, Deelen, Joris, Mangino, Massimo, Willemsen, Gonneke, Albrecht, Eva, Amin, Najaf, Beekman, Marian, de Geus, Eco J C, Henders, Anjali, Nelson, Christopher P, Steves, Claire J, Wright, Margie J, de Craen, Anton J M, Isaacs, Aaron, Matthews, Mary, Moayyeri, Alireza, Montgomery, Grant W, Oostra, Ben A, Vink, Jacqueline M, Spector, Tim D, Slagboom, P Eline, Martin, Nicholas G, Samani, Nilesh J, van Duijn, Cornelia M, Boomsma, Dorret I

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The Challenges of Genome-Wide Interaction Studies: Lessons to Learn from the Analysis of HDL Blood Levels 由 van Leeuwen, Elisabeth M., Smouter, Françoise A. S., Kam-Thong, Tony, Karbalai, Nazanin, Smith, Albert V., Harris, Tamara B., Launer, Lenore J., Sitlani, Colleen M., Li, Guo, Brody, Jennifer A., Bis, Joshua C., White, Charles C., Jaiswal, Alok, Oostra, Ben A., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G., Boerwinkle, Eric, Ballantyne, Christie M., Gudnason, Vilmundur, Psaty, Bruce M., Cupples, L. Adrienne, Järvelin, Marjo-Riitta, Ripatti, Samuli, Isaacs, Aaron, Müller-Myhsok, Bertram, Karssen, Lennart C., van Duijn, Cornelia M.

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Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis 由 Johansson, Åsa, Marroni, Fabio, Hayward, Caroline, Franklin, Christopher S., Kirichenko, Anatoly V., Jonasson, Inger, Hicks, Andrew A., Vitart, Veronique, Isaacs, Aaron, Axenovich, Tatiana, Campbell, Susan, Dunlop, Malcolm G., Floyd, Jamie, Hastie, Nick, Hofman, Albert, Knott, Sara, Kolcic, Ivana, Pichler, Irene, Polasek, Ozren, Rivadeneira, Fernando, Tenesa, Albert, Uitterlinden, André G., Wild, Sarah H., Zorkoltseva, Irina V., Meitinger, Thomas, Wilson, James F., Rudan, Igor, Campbell, Harry, Pattaro, Cristian, Pramstaller, Peter, Oostra, Ben A., Wright, Alan F., van Duijn, Cornelia M., Aulchenko, Yurii S., Gyllensten, Ulf

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Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram 由 Verweij, Niek, Mateo Leach, Irene, Isaacs, Aaron, Arking, Dan E., Bis, Joshua C., Pers, Tune H., Van Den Berg, Marten E., Lyytikäinen, Leo-Pekka, Barnett, Phil, Wang, Xinchen, Soliman, Elsayed Z., Van Duijn, Cornelia M., Kähönen, Mika, Van Veldhuisen, Dirk J., Kors, Jan A., Raitakari, Olli T., Silva, Claudia T., Lehtimäki, Terho, Hillege, Hans L., Hirschhorn, Joel N., Boyer, Laurie A., Van Gilst, Wiek H., Alonso, Alvaro, Sotoodehnia, Nona, Eijgelsheim, Mark, De Boer, Rudolf A., De Bakker, Paul I. W., Franke, Lude, Van Der Harst, Pim

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